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汉坦病毒核衣壳蛋白在病毒糖蛋白细胞内运输中的作用。

Role of nucleocapsid protein of hantaviruses in intracellular traffic of viral glycoproteins.

机构信息

Department of Microbiology, Hokkaido University Graduate School of Medicine, Kita-15, Nishi-7, Kita-ku, Sapporo 060-8638, Japan.

出版信息

Virus Res. 2013 Dec 26;178(2):349-56. doi: 10.1016/j.virusres.2013.09.022. Epub 2013 Sep 23.

Abstract

To understand the role of nucleocapsid protein (NP) of hantaviruses in viral assembly, the effect of NP on intracellular traffic of viral glycoproteins Gn and Gc was investigated. Double staining of viral and host proteins in Hantaan virus (HTNV)-infected Vero E6 cells showed that Gn and Gc were localized to cis-Golgi, in which virus particles are thought to be formed. When HTNV Gn and Gc were expressed by a plasmid encoding glycoprotein precursor (GPC), which is posttranslationally cleaved into Gn and Gc, Gn was localized to cis-Golgi, whereas Gc showed diffuse distribution in the cytoplasm in 32.9% of Gc-positive cells. The ratio of the diffused Gc-positive cells was significantly decreased to 15.0% by co-expression of HTNV NP. Co-expression of HTNV GPC with NPs of other hantaviruses, such as Seoul virus, Puumala virus and Sin Nombre virus, also reduced the ratios of diffused Gc-positive cells to 13.5%, 25.2%, and 11.6%, respectively. Among amino- and carboxyl-terminally truncated HTNV NPs, NP75-429, NP116-429, NP1-333, NP1-233, and NP1-155 possessed activity to reduce the ratio of diffused Gc-positive cells, while NP155-429 and NP1-116 did not. NP30-429 has partial activity. These results indicate that amino acid region 116-155 of NP is important for the activity, although amino acid region 1-30 is partially related. Truncation of the HTNV Gc cytoplasmic tail caused an increase in diffused Gc-positive cells. In addition, the effect of coexpression of HTNV NP was weakened. These results suggest that HTNV NP has a role to promote Golgi localization of Gc through a mechanism possibly mediated by the Gc cytoplasmic tail.

摘要

为了了解汉坦病毒核衣壳蛋白(NP)在病毒组装中的作用,研究了 NP 对病毒糖蛋白 Gn 和 Gc 细胞内运输的影响。汉坦病毒(HTNV)感染的 Vero E6 细胞中病毒和宿主蛋白的双重染色显示,Gn 和 Gc 定位于顺式高尔基体,病毒颗粒被认为在此形成。当 HTNV Gn 和 Gc 由编码糖蛋白前体(GPC)的质粒表达时,GPC 在翻译后被切割成 Gn 和 Gc,Gn 定位于顺式高尔基体,而 Gc 在 32.9%的 Gc 阳性细胞中呈现弥散分布。通过共表达 HTNV NP,弥散的 Gc 阳性细胞的比例显著降低至 15.0%。与其他汉坦病毒如首尔病毒、普马拉病毒和辛诺伯病毒的 NP 共表达 HTNV GPC 也分别将弥散的 Gc 阳性细胞的比例降低至 13.5%、25.2%和 11.6%。在氨基和羧基端截断的 HTNV NPs 中,NP75-429、NP116-429、NP1-333、NP1-233 和 NP1-155 具有降低弥散的 Gc 阳性细胞比例的活性,而 NP155-429 和 NP1-116 则没有。NP30-429 具有部分活性。这些结果表明,NP 的氨基酸区域 116-155 对于该活性很重要,尽管氨基酸区域 1-30 部分相关。HTNV Gc 细胞质尾巴的截断导致弥散的 Gc 阳性细胞增加。此外,共表达 HTNV NP 的效果减弱。这些结果表明,HTNV NP 通过可能由 Gc 细胞质尾巴介导的机制发挥作用,促进 Gc 的高尔基体定位。

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